Polymeric Material for Container

ABSTRACT

A formulation for producing a polymeric material including polypropylene, a chemical blowing agent, and optional components as described.

PRIORITY CLAIM

This application is a continuation of U.S. application Ser. No.15/713,799, filed Sep. 25, 2017, which is a continuation of U.S.application Ser. No. 14/468,789, filed Aug. 26, 2014, which claimspriority under 35 U.S.C. § 119(e) to U.S. Provisional Application Ser.No. 61/869,928, filed Aug. 26, 2013, each of which is expresslyincorporated by reference herein.

BACKGROUND

The present disclosure relates to polymeric materials that can be formedto produce a container, and in particular, polymeric materials thatinsulate. More particularly, the present disclosure relates topolymer-based formulations that can be formed to produce an insulatednon-aromatic polymeric material.

SUMMARY

According to the present disclosure, a polymeric material includes apolymeric resin and cell-forming agents. In illustrative embodiments, ablend of polymeric resins and cell-forming agents is mixed and extrudedor otherwise formed to produce an insulated non-aromatic polymericmaterial.

In illustrative embodiments, an insulative cellular non-aromaticpolymeric material produced in accordance with the present disclosurecan be formed to produce an insulative cup or container. Polypropyleneresin is used to form the insulative cellular non-aromatic polymericmaterial in illustrative embodiments.

In illustrative embodiments, an insulative cellular non-aromaticpolymeric material comprises one or more of the following, apolypropylene base resin having high melt strength, polypropylenecopolymer or homopolymer, and cell-forming agents. The cell-formingagents include at least one of the following, a chemical nucleatingagent and a physical blowing agent.

In illustrative embodiments, a polypropylene-based formulation inaccordance with the present disclosure is heated and extruded to producea tubular extrudate (in an extrusion process) that can be formed toprovide a strip of insulative cellular non-aromatic polymeric material.A physical blowing agent in the form of an inert gas is introduced intoa molten resin before the tubular extrudate is formed.

In illustrative embodiments, the insulative cellular non-aromaticpolymeric material has a density of less than about 0.6 grams per cubiccentimeter. In illustrative embodiments, the insulative cellularnon-aromatic polymeric material has a density in a range of about 0.2grams per cubic centimeter to about 0.6 grams per cubic centimeter. Inillustrative embodiments, the insulative cellular non-aromatic polymericmaterial has a density in a range of about 0.3 grams per cubiccentimeter to about 0.5 grams per cubic centimeter.

Additional features of the present disclosure will become apparent tothose skilled in the art upon consideration of illustrative embodimentsexemplifying the best mode of carrying out the disclosure as presentlyperceived.

BRIEF DESCRIPTIONS OF THE DRAWINGS

The detailed description particularly refers to the accompanying FIGUREin which:

FIG. 1 is a perspective view of an unassembled density determinationapparatus showing the components (clockwise starting in the upper left)gem holder, platform, suspension bracket, and suspension spacer.

DETAILED DESCRIPTION

An insulative cellular non-aromatic polymeric material produced inaccordance with the present disclosure can be formed to produce aninsulative container such as an insulative cup. As an example, theinsulative cellular non-aromatic polymeric material comprises apolypropylene base resin and one or more cell-forming agents. In oneillustrative example, the insulative cellular non-aromatic polymericmaterial is located between and coupled to an inner polymeric layer andan outer polymeric layer to produce a multi-layer tube or multi-layerparison that is blow molded to form an insulative container.

A material-formulation process in accordance with the present disclosureuses a polypropylene-based formulation to produce a strip of insulativecellular non-aromatic polymeric material. The polypropylene-basedformulation is heated in an extruder where a cell-forming agent isintroduced into the molten formulation prior to extrusion of thematerials from the extruder. As the molten materials exit the extruder,cells nucleate in the molten material and the material expands to formthe sheet of insulative cellular non-aromatic polymeric material.

In one exemplary embodiment, a formulation used to produce theinsulative cellular non-aromatic polymeric material includes at leastone polymeric material. The polymeric material may include one or morebase resins. In one example, the base resin is polypropylene. In anillustrative embodiment, a base resin can include DAPLOY™ WB140HMSpolypropylene homopolymer available from Borealis AG of Vienna, Austria.In another illustrative embodiment, a base resin can include BraskemF020HC polypropylene homopolymer available from Braskem of Philadelphia,Pa. In an embodiment, a base resin can include both DAPLOY™ WB140HMSpolypropylene homopolymer and Braskem F020HC polypropylene homopolymer.

In embodiments with more than one polypropylene copolymer base resin,different polypropylene copolymers can be used depending on theattributes desired in the formulation. Depending on the desiredcharacteristics, the ratio of two polypropylene resins may be varied,e.g., 20%/80%, 25%/75%, 30%/70%, 35%/65%, 40%/60%, 45%/55%, 50%/50%,etc. In an embodiment, a formulation includes three polypropylene resinsin the base resin. Again, depending on the desired characteristics, thepercentage of three polypropylene resins can be varied, 33%/33%/33%,30%/30%/40%, 25%/25%/50%, etc.

In an illustrative embodiment, a formulation includes one or more baseresins. The amount of one or more base resins may be one of severaldifferent values or fall within several different ranges. It is withinthe scope of the present disclosure to select an amount of polypropyleneto be one of the following values: about of 85%, 86%, 87%, 88%, 89%,90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99%, 99.5%, and 99.9% ofthe total formulation by weight percentage. In a first set of ranges,the range of polypropylene base resin is one of the following ranges:about 85% to 90%, 85% to 92%, 85% to 95%, 85% to 96%, 85% to 97%, 85% to98%, 85% to 99%, and 85% to 99.9% of the total formulation by weightpercentage. In a second set of ranges, the range of polypropylene baseresin is one of the following ranges: about 90 to 99.9%, 92% to 99.9%,95% to 99.9%, 96% to 99.9%, 97% to 99.9%, 98% to 99.9%, and 99% to 99.9%of the total formulation by weight percentage. In a third set of ranges,the range of polypropylene base resin is one of the following ranges:about 87.5% to 95%, 87.5% to 96%, 95% to 99%, and 96% to 99% of thetotal formulation by weight percentage. The values and ranges areembodied in Examples 1 to 8.

In an embodiment, an insulative cellular non-aromatic polymeric materialincludes multiple layers. In an embodiment, a polymeric material asdisclosed herein has an outer exterior skin layer in addition to thecore layer of at least one base resin. In an embodiment, a polymericmaterial as disclosed herein has an inner exterior skin layer inaddition to the core layer of at least one base resin. In an embodiment,a polymeric material includes both an exterior skin layer and an innerexterior skin layer in addition to the core layer of at least one baseresin. In an embodiment, the outer skin layer can be polypropylene orpolyethylene. In an embodiment, the inner skin layer can bepolypropylene or polyethylene. In an embodiment where a polymericmaterial includes both an inner and outer skin layer in addition to thecore layer of at least one base resin, the inner and outer skin layerscan each be independently polypropylene or polyethylene.

In an embodiment, a skin layer comprising polypropylene can be a highstiffness polypropylene. In another illustrative embodiment, a skinlayer comprising polypropylene can be a high impact polypropylene. In anembodiment, a skin layer comprising polypropylene can be DOW® D 207.03developmental performance polypropylene resin. In an embodiment, a skinlayer comprising polypropylene can be DOW® DC 7067.00 polypropyleneimpact copolymer. In an embodiment, an outer, inner, or both outer andinner skin layer can be solid or cellular (i.e., foamed). In anillustrative embodiment, the density of a skin layer (inner and/orouter) can be about 0.9 g/cm³.

In an embodiment, either of the outer or inner skin layer can be apolyethylene. In an illustrative embodiment, the outer skin layer, theinner skin layer, or both the outer and inner skin layer includes a highdensity ethylene hexane-1 copolymer such as Chevron Phillips MARLEX® HHM5502 BN.

Long chain branching refers to the presence of polymer side chains(branches) that have a length that is comparable or greater than alength of the backbone to which the polymer side chains are coupled.Long chain branching creates viscoelastic chain entanglements (polymerentanglements) that hamper flow during extensional or orientedstretching and provide for a strain hardening phenomenon. The strainhardening phenomenon may be observed through two analytical methods.

The first analytical method used to observe the presence of strainhardening on an extensional rheometer. During extensional or orientedflow on an extensional rheometer, strain hardening will occur whenpolymer entanglements do not allow the polymer to flow under LinearViscoelastic (LVE) conditions. As a result, these polymer entanglementshamper flow and create a deviation from the LVE conditions as observedas a hook formation. The strain hardening phenomenon becomes more severeas strain and strain rate increase due to faster and more severe polymerchain entanglement motion. Virgin polymers without long chain branchingwill exhibit LVE flow characteristics. In comparison, long chainbranched polymers will exhibit strain hardening and which causes adeviation from the LVE flow characteristics of the virgin polymerproviding the hook formation under the same test conditions.

The second analytical method used to observe the presence of long chainbranching is evaluating melt strength data as tested per ISO 16790 whichis incorporated by reference herein in its entirety. An amount of meltstrength is known to be directly related to the presence of long chainbranching when compared to similar virgin polymers lacking long chainbranching. By way of example, Borealis DAPLOY™ WB140HMS Polypropylene(PP) (available from Borealis AG) is compared to other polymers havingsimilar molecular weight, polydispersity index, and other physicalcharacteristics. The DAPLOY™ WB140HMS PP has a melt strength whichexceeds about 36 cN while other similar PP resins lacking long chainbranching have a melt strength of less than about 10 cN.

The formulation used to produce the insulative cellular non-aromaticpolymeric material may further include one or more cell-forming agents.Cell-forming agents include nucleating agents and blowing agents. Anucleating agent is used to provide and control nucleation sites withina molten formulation to promote formation of cells, bubbles, or voids inthe molten formulation during extrusion. A blowing agent is used to growcells in the molten material at nucleation sites. Blowing agents may beused alone in the formulation or with nucleating agents.

Nucleating agent means a chemical or physical material that providessites for cells to form in a molten formulation mixture. Nucleatingagents may include chemical nucleating agents and physical nucleatingagents. The nucleating agent may be blended with the formulation that isintroduced into the hopper of the extruder. Alternatively, thenucleating agent may be added to the molten resin mixture in theextruder.

Suitable physical nucleating agents have desirable particle size, aspectratio, and top-cut properties. Examples include, but are not limited to,talc, CaCO₃, mica, and mixtures of at least two of the foregoing. Onerepresentative example is Heritage Plastics HT6000 Linear Low DensityPolyethylene (LLDPE) Based Talc Concentrate.

In an illustrative embodiment, a formulation includes a physicalnucleating agent (e.g., talc). The amount of a physical nucleating agentmay be one of several different values or fall within several differentranges. It is within the scope of the present disclosure to select anamount of a physical nucleating agent to be one of the following values:about 0%, 0.1%, 0.25%, 0.5%, 0.75%, 1%, 1.5%, 2%, 2.5%, 3%, 4%, 5%, 6%,and 7% of the total formulation by weight percentage. In a first set ofranges, the range of physical nucleating agent is one of the followingranges: about 0% to 7%, 0.1% to 7%, 0.25% to 7%, 0.5% to 7%, 0.75% to7%, 1% to 7%, 1.5% to 7%, 2% to 7%, 2.5% to 7%, 3% to 7%, 4% to 7%, 5%to 7%, and 6% to 7% of the total formulation by weight percentage. In asecond set of ranges, the range of physical nucleating agent is one ofthe following ranges: about 0% to 6%, 0% to 5%, 0% to 4%, 0% to 3%, 0%to 2.5%, 0% to 2%, 0% to 1.5%, 0% to 1%, 0% to 0.75%, 0% to 0.5%, 0% to0.25%, and 0% to 0.1% of the total formulation by weight percentage. Ina third set of ranges, the range of physical nucleating agent is one ofthe following ranges: about 0.1% to 6%, 0.1% to 5%, 0.1% to 4%, 0.1% to3%, 0.1% to 2.5%, 0.1% to 2%, 0.1% to 1.5%, 0.1% to 1%, 0.1% to 0.75%,0.1% to 0.5%, and 0.1% to 0.25% of the total formulation by weightpercentage. The values and ranges are embodied in Examples 1 to 8. In anembodiment, the formulation lacks talc.

Suitable chemical nucleating agents decompose to create cells in themolten formulation when a chemical reaction temperature is reached.These small cells act as nucleation sites for larger cell growth from aphysical or other type of blowing agent. In one example, the chemicalnucleating agent is citric acid or a citric acid-based material. Onerepresentative example is HYDROCEROL™ CF-40E (available from ClariantCorporation), which contains citric acid and a crystal nucleating agent.

In an illustrative embodiment, a formulation includes a nucleatingagent. The amount of a nucleating agent may be one of several differentvalues or fall within several different ranges. It is within the scopeof the present disclosure to select an amount of a nucleating agent tobe one of the following values: about 0.1%, 0.25%, 0.5%, 0.75%, 1%,1.5%, 2%, 2.5%, 3%, 4%, 5%, 10%, and 15% of the total formulation byweight percentage. In a first set of ranges, the range of nucleatingagent is one of the following ranges: about 0.1% to 15%, 0.25% to 15%,0.5% to 15%, 0.75% to 15%, 1% to 15%, 1.5% to 15%, 2% to 15%, 2.5% to15%, 3% to 15%, 4% to 15%, 5% to 15%, and 10% to 15% of the totalformulation by weight percentage. In a second set of ranges, the rangeof nucleating agent is one of the following ranges: about 0.1% to 10%,0.25% to 10%, 0.5% to 10%, 0.75% to 10%, 1% to 10%, 1.5% to 10%, 2% to10%, 2.5% to 10%, 3% to 10%, 4% to 10%, and 5% to 10% of the totalformulation by weight percentage. In a third set of ranges, the range ofnucleating agent is one of the following ranges: about 0.1% to 5%, 0.25%to 5%, 0.5% to 5%, 0.75% to 5%, 1% to 5%, 1.5% to 5%, 2% to 5%, 2.5% to5%, 3% to 5%, and 4% to 5% of the total formulation by weightpercentage. The values and ranges are embodied in Examples 1 to 8.

A blowing agent refers to a physical or a chemical material (orcombination of materials) that acts to expand nucleation sites. Blowingagents may include chemical blowing agents, physical blowing agents,combinations thereof, or several types of chemical and physical blowingagents. The blowing agent acts to reduce density by forming cells in themolten formulation at the nucleation sites. The blowing agent may beadded to the molten resin mixture in the extruder.

Chemical blowing agents are materials that degrade or react to produce agas. Chemical blowing agents may be endothermic or exothermic. Chemicalblowing agents typically degrade at a certain temperature to decomposeand release gas. One example of a chemical blowing agent is citric acidor citric-based material. One representative example is HYDROCEROL™CF-40E (available from Clariant Corporation), which contains citric acidand a crystal nucleating agent. Here, the citric acid decomposes at theappropriate temperature in the molten formulation and forms a gas whichmigrates toward the nucleation sites and grows cells in the moltenformulation. If sufficient chemical blowing agent is present, thechemical blowing agent may act as both the nucleating agent and theblowing agent.

In another example, chemical blowing agents may be selected from thegroup consisting of azodicarbonamide; azodiisobutyro-nitrile;benzenesulfonhydrazide; 4,4-oxybenzene sulfonylsemicarbazide; p-toluenesulfonyl semi-carbazide; barium azodicarboxylate;N,N′-dimethyl-N,N′-dinitrosoterephthalamide; trihydrazino triazine;methane; ethane; propane; n-butane; isobutane; n-pentane; isopentane;neopentane; methyl fluoride; perfluoromethane; ethyl fluoride;1,1-difluoroethane; 1,1,1-trifluoroethane; 1,1,1,2-tetrafluoro-ethane;pentafluoroethane; perfluoroethane; 2,2-difluoropropane;1,1,1-trifluoropropane; perfluoropropane; perfluorobutane;perfluorocyclobutane; methyl chloride; methylene chloride; ethylchloride; 1,1,1-trichloroethane; 1,1-dichloro-1-fluoroethane;1-chloro-1,1-difluoroethane; 1,1-dichloro-2,2,2-trifluoroethane;1-chloro-1,2,2,2-tetrafluoroethane; trichloromonofluoromethane;dichlorodifluoromethane; trichlorotrifluoroethane;dichlorotetrafluoroethane; chloroheptafluoropropane;dichlorohexafluoropropane; methanol; ethanol; n-propanol; isopropanol;sodium bicarbonate; sodium carbonate; ammonium bicarbonate; ammoniumcarbonate; ammonium nitrite;N,N′-dimethyl-N,N′-dinitrosoterephthalamide;N,N′-dinitrosopentamethylene tetramine; azodicarbonamide;azobisisobutylonitrile; azocyclohexylnitrile; azodiaminobenzene;bariumazodicarboxylate; benzene sulfonyl hydrazide; toluene sulfonylhydrazide; p,p′-oxybis(benzene sulfonyl hydrazide); diphenylsulfone-3,3′-disulfonyl hydrazide; calcium azide; 4,4′-diphenyldisulfonyl azide; p-toluene sulfonyl azide, and combinations thereof.

In one aspect of the present disclosure, where a chemical blowing agentis used, the chemical blowing agent may be introduced into the materialformulation that is added to the hopper.

One example of a physical blowing agent is nitrogen (N₂). The N₂ ispumped into the molten formulation via a port in the extruder as asupercritical fluid. The molten material with the N₂ in suspension thenexits the extruder via a die where a pressure drop occurs. As thepressure drop happens, N₂ moves out of suspension toward the nucleationsites where cells grow. Excess gas blows off after extrusion with theremaining gas trapped in the cells formed in the extrudate. Othersuitable examples of physical blowing agents include, but are notlimited to, carbon dioxide (CO₂), helium, argon, or air. Physicalblowing agents may also include mixtures of alkanes such as, but notlimited to, pentane, butane, and the like. In an illustrative example, aphysical blowing agent may be introduced at a rate of about 0.07 poundsper hour to about 0.1 pounds per hour. In another illustrative example,the physical blowing agent may be introduced at a rate of about 0.74pounds per hour to about 0.1 pounds per hour. In another illustrativeexample, the physical blowing agent may be introduced at a rate of about0.75 to about 0.1 pounds per hour.

In one aspect of the present disclosure, at least one slip agent may beincorporated into the formulation to aid in increasing production rates.Slip agent (also known as a process aid) is a term used to describe ageneral class of materials which are added to the formulation andprovide surface lubrication to the polymer during and after conversion.Slip agents may also reduce or eliminate die drool. Representativeexamples of slip agent materials include amides of fats or fatty acids,such as, but not limited to, erucamide and oleamide. In one exemplaryaspect, amides from oleyl (single unsaturated C-18) through erucyl (C-22single unsaturated) may be used. Other representative examples of slipagent materials include low molecular weight amides andfluoroelastomers. Combinations of two or more slip agents can be used.Slip agents may be provided in a master batch pellet form and blendedwith the resin formulation. One example of a slip agent is commerciallyavailable as AMPACET™ 102109 Slip PE MB. Another example of a slip agentthat is commercially available is AMAPACET™ 102823 Process Aid PE MB.

In an illustrative embodiment, a formulation includes a slip agent. Theamount of a slip agent may be one of several different values or fallwithin several different ranges. It is within the scope of the presentdisclosure to select an amount of a slip agent to be one of thefollowing values: about 0%, 0.1%, 0.25%, 0.5%, 0.75%, 1%, 1.5%, 2%,2.5%, and 3% of the total formulation by weight percentage. In a firstset of ranges, the range of slip agent is one of the following ranges:about 0% to 3%, 0.1% to 3%, 0.25% to 3%, 0.5% to 3%, 0.75% to 3%, 1% to3%, 1.5% to 3%, 2% to 3%, and 2.5% to 3% of the total formulation byweight percentage. In a second set of ranges, the range of slip agent isone of the following ranges: about 0% to 2.5%, 0% to 2%, 0% to 1.5%, 0%to 1%, 0% to 0.75%, 0% to 0.5%, 0% to 0.25%, and 0% to 0.1% of the totalformulation by weight percentage. In a third set of ranges, the range ofslip agent is one of the following ranges: about 0.1% to 2.5%, 0.1% to2%, 0.1% to 1.5%, 0.1% to 1%, 0.1% to 0.75%, 0.1% to 0.5%, and 0.1% to0.25% of the total formulation by weight percentage. The values andranges are embodied in Examples 1 to 8. In an embodiment, theformulation lacks a slip agent.

In another aspect of the present disclosure, an impact modifier may beincorporated into the formulation to minimize fracturing of theinsulative cellular non-aromatic polymeric material when subjected to animpact such as a drop test. One representative example of a suitableimpact modifier is DOW® AFFINITY™ PL 1880G polyolefin plastomer.

In an illustrative embodiment, a formulation includes a colorant. Theamount of a colorant may be one of several different values or fallwithin several different ranges. It is within the scope of the presentdisclosure to select an amount of a colorant to be one of the followingvalues: about 0%, 0.1%, 0.25%, 0.5%, 0.75%, 1%, 1.5%, 2%, 2.5%, 3%, and4% of the total formulation by weight percentage. In a first set ofranges, the range of colorant is one of the following ranges: about 0%to 4%, 0.1% to 4%, 0.25% to 4%, 0.5% to 4%, 0.75% to 4%, 1% to 4%, 1.5%to 4%, 2% to 4%, 2.5% to 4%, and 3% to 4% of the total formulation byweight percentage. In a second set of ranges, the range of colorant isone of the following ranges: about 0% to 3%, 0% to 2.5%, 0% to 2%, 0% to1.5%, 0% to 1%, 0% to 0.75%, 0% to 0.5%, 0% to 0.25%, and 0% to 0.1% ofthe total formulation by weight percentage. In a third set of ranges,the range of colorant is one of the following ranges: about 0.1% to2.5%, 0.1% to 2%, 0.1% to 1.5%, 0.1% to 1%, 0.1% to 0.75%, 0.1% to 0.5%,and 0.1% to 0.25% of the total formulation by weight percentage. Thevalues and ranges are embodied in Examples 1 to 8. In an embodiment, theformulation lacks a colorant.

One or more additional components and additives optionally may beincorporated, such as, but not limited to, colorants (such as, but notlimited to, titanium dioxide), and compound regrind.

In an embodiment, the insulative cellular non-aromatic polymericmaterial is located between and coupled to an inner polymeric layer andan outer polymeric layer to produce a multi-layer tube. For example, themulti-layer tube can be a bottle. In an embodiment, the insulativecellular non-aromatic polymeric material is located between and coupledto an inner polymeric layer and an outer polymeric layer to produce amulti-layer tube. For example, the multi-layer tube can be a bottle. Itis within the scope of the present disclosure to select a bottle densityto be one of the following values: about 0.5, 0.6, 0.65, 0.7, 0.75, 0.8,0.9, 0.92, and 1 g/cm³. In a first set of ranges, the range of densityis one of the following ranges: about 0.5 to 0.92, 0.6 to 0.92, 0.7 to0.92, 0.75 to 0.92, 0.8 to 0.92, and 0.5 to 1 g/cm³ of the totalformulation by weight percentage. In a second set of ranges, the rangeof density is one of the following ranges: about 0.5 to 0.9, 0.6 to 0.9,0.7 to 0.9, 0.75 to 0.9, and 0.8 to 0.9 g/cm³ of the total formulationby weight percentage. In a third set of ranges, the range of density isone of the following ranges: about 0.7 to 0.85, 0.7 to about 0.8, 0.72to about 0.85, and 0.75 to 0.85 g/cm³ of the total formulation by weightpercentage. Density was determined according to the density testprocedure outlined in Example 8.

In an embodiment, the insulative cellular non-aromatic polymericmaterial is located between and coupled to an inner polymeric layer andan outer polymeric layer to produce a multi-layer parison. It is withinthe scope of the present disclosure to select a multi-layer parison tobe one of the following values: about 0.4, 0.45, 0.5, 0.55, 0.6, 0.65,0.7, 0.75, and g/cm³. In a first set of ranges, the range of density isone of the following ranges: about 0.4 to 0.8, 0.45 to 0.8, 0.5 to 0.8,0.55 to 0.8, 0.6 to 0.8, 0.65 to 0.8, 0.7 to 0.8, and 0.75 to 0.8 g/cm³of the total formulation by weight percentage. In a second set ofranges, the range of density is one of the following ranges: about 0.4to 0.7, 0.45 to 0.7, 0.5 to 0.7, 0.55 to 0.7, 0.6 to 0.7, and 0.65 to0.7 g/cm³ of the total formulation by weight percentage. In a third setof ranges, the range of density is one of the following ranges: about0.4 to 0.6, 0.5 to 0.6, and 0.4 to 0.5 g/cm³ of the total formulation byweight percentage. Density was determined according to the density testprocedure outlined in Example 8.

Before the drop test is performed, the insulative cellular non-aromaticpolymeric material is coupled and located between two polymeric layersto form a multi-layer parison. The multi-layer parison is then formed,for example, via blow molding into a container. The resulting containeris then tested according to one of the Plastic Bottle Institute Test forDrop Impact Resistance of Plastic Bottles, PBI 4-1968, Rev. 2-1988 testmethod and the Rigid Plastics Container Division of the The Society ofPlastics Industry, Inc. RPCD-7-1991 test method.

In another example, the drop test may be performed according to thefollowing procedure. The container is filled with water and closed offwith, for example, a lid. The sample container is then held at about 73degrees Fahrenheit (22.8 degrees Celsius) and about 50% relativehumidity. The filled, capped containers are then subjected to thefollowing procedure: (a) the filled, capped container is located atabout five feet above a hard surface such as concrete or tile; (b) thefilled, capped container is then oriented such that a bottom of thefilled, capped container is arranged to lie in a substantially parallelrelation to the hard surface; (c) each of ten capped, filled containersare dropped; (d) upon impact, each filled, capped container is examinedfor any break or shattering of the wall that causes water to leak out ofthe bottle; and (d) the total number of bottles showing any sign ofleakage after the drop test are counted as failures.

According to an aspect of the present disclosure, there is provided amethod of forming a multi-later parison formed from insulative cellularnon-aromatic polymeric material, the method comprising the steps of:

-   -   a) heating, to a molten state, a mixture comprising:    -   at least 85% (w/w) of at least one polypropylene base resin;    -   0-15% (w/w) of at least one chemical nucleating agent; and    -   0-3% (w/w) of a slip agent;    -   b) injecting a blowing agent into the molten mixture;    -   c) extruding the molten mixture resulting from step b) to form a        core layer, wherein said mixture is co-extruded with an outer        skin layer to form a multi-layer parison.

The core layer and outer skin layer forming the multi-layer parison aredisposed one directly on top of the other, in the sense that the corelayer and outer skin layers are coupled to one another.

In an embodiment, step c) is performed without the use of a tandemextruder arrangement.

In another embodiment, step c) comprises extruding the molten mixtureresulting from step b) to form a core layer, wherein said mixture isco-extruded with an outer skin layer and an inner skin layer to form amulti-layer parison. Where the multi-layer parison comprises both outerand inner skin layers, it will be understood that the core layer isdisposed between said outer an inner skin layers, such that a firstsurface of the core layer is coupled to the outer skin layer, and asecond surface of the core layer opposite the said first surface iscoupled to said inner skin layer.

In another embodiment, step c) further comprises co-extruding any numberof additional layers with the core layer and the outer skin layer.

In another embodiment, the outer and inner skin layers each comprisepolypropylene or polyethylene.

In one example, the polypropylene used in either of the skin layers is ahigh stiffness polypropylene. In another example, the polypropylene usedin either of the skin layers is a high impact polypropylene. In anotherexample, the polypropylene used in either of the skin layers is DOW® D207.03 developmental performance polypropylene resin or DOW® DC 7067.00polypropylene impact copolymer.

In one example, the polyethylene used in either of the skin layers is ahigh density ethylene hexane-1 copolymer. In another example, thepolyethylene used in either of the skin layers is Chevron PhillipsMARLEX® HHM 5502 BN.

In one example, both of the outer and inner skin layers are a formedfrom a polypropylene selected from DOW® D 207.03 developmentalperformance polypropylene resin or DOW® DC 7067.00 polypropylene impactcopolymer.

In example, the mixture of step a) is

-   -   79-82% (w/w) of a first polypropylene homopolymer;    -   14-16% (w/w) of a second polypropylene homopolymer;    -   0.01-1.5% (w/w) of a chemical nucleating agent;    -   1-3% (w/w) of a slip agent; and    -   0.1-1% (w/w) of a physical nucleating agent.

In another embodiment, the method further comprises a step d) ofblow-molding the multi-layer parison resulting from step c) to provide acontainer formed from insulative cellular non-aromatic polymericmaterial.

According to another aspect of the present disclosure, there is provideda method of forming a multi-later parison formed from insulativecellular non-aromatic polymeric material, the method comprising thesteps of:

-   -   a) heating, to a molten state, a mixture comprising:    -   at least 85% (w/w) of at least one polypropylene base resin;    -   0-15% (w/w) of at least one chemical nucleating agent; and    -   0-3% (w/w) of a slip agent;    -   b) injecting a blowing agent into the molten mixture;    -   c) extruding the molten mixture resulting from step b) to form a        core layer, wherein said mixture is co-extruded with an outer        skin layer to form a multi-layer parison; and    -   d) blow-molding the multi-layer parison resulting from step c)        to provide a container formed from insulative cellular        non-aromatic polymeric material.

According to another aspect of the present disclosure, there is provideda multi-layer parison obtainable, obtained, or directly obtained by aprocess defined herein.

According to another aspect of the present invention, there is provideda container obtainable, obtained, or directly obtained by a processdefined herein.

Example 1 Formulation and Extrusion

In the mono-layer, Borealis WB140HMS polypropylene homopolymer was usedas the primary polypropylene base resin. Braskem F020HC polypropylenehomopolymer was used as the secondary polypropylene base resin. Theresins were blended with Hydrocerol CF-40E as the primary nucleationagent, Heritage Plastics HT4HP talc as a secondary nucleation agent,Ampacet 102823 Process Aid PE MB LLDPE as a slip agent, Colortech11933-19 colorant, and N₂ as the blowing agent. The percentages were:

81.4%  Borealis WB140 HMS polypropylene homopolymer  15% Braskem F020HCpolypropylene homopolymer 0.1% Hydrocerol CF-40E Chemical Blowing Agent 2% Ampacet 102823 Process Aid PE MB LLDPE  1% Colortech 11933-19Titanium Oxide 0.5% Heritage Plastics HT4HP Talc

The formulation was added to an extruder hopper. The extruder heated theformulation to form a molten resin mixture.

The N₂ was injected at about 0.0751 lbs/hr and about 0.0750 lbs/hr intothe resin blend to expand the resin and reduce density. The mixture thusformed was extruded through a die head into a parison. The parison wasthen blow molded with air to form a container.

Containers were formed from a monolayer tube. A monolayer tube used toform insulative cellular non-aromatic polymeric bottle had a density ofabout 0.670 grams per cubic centimeter when both about 0.0751 lbs/hr andabout 0.0750 lbs/hr of N₂ were added to the molten resin mixture.

Example 2 Formulation and Extrusion

In a core layer, Borealis WB140HMS polypropylene homopolymer was used asthe primary polypropylene base resin. Braskem F020HC polypropylenehomopolymer was used as the secondary polypropylene base resin. Theresins were blended with Hydrocerol CF-40E as the primary nucleationagent, Heritage Plastics HT4HP talc as a secondary nucleation agent,Ampacet 102823 Process Aid PE MB LLDPE as a slip agent, Colortech11933-19 colorant, and N₂ as the blowing agent. The percentages were:

81.45%    Borealis WB140 HMS polypropylene homopolymer 15%  BraskemF020HC polypropylene homopolymer 0.05%   Hydrocerol CF-40E ChemicalBlowing Agent 2% Ampacet 102823 Process Aid PE MB LLDPE 1% Colortech11933-19 Titanium Oxide 0.5%  Heritage Plastics HT4HP Talc

The formulation was added to an extruder hopper. The extruder heated theformulation to form a molten resin mixture. The N₂ was injected at about0.075 lbs/hr into the resin blend to expand the resin and reducedensity.

The mixture thus formed was communicated to a co-extrusion die where themixture was extruded to form a core layer along with an outer skin layerto establish a multi-layer parison. The multi-layer parison was thenblow molded with air to form a container. In one example, the outer skincomprises a polypropylene resin. In another example, the outer skin wascomprised of DOW® DC 7067.00 polypropylene impact copolymer.

The multi-layer parison was then blow molded to form an insulativecellular non-aromatic polymeric bottle which had a bottle density ofabout 0.7 grams per cubic centimeter and the core layer had a density ofabout 0.665 grams per cubic centimeter.

Example 3 Formulation and Extrusion

In a core layer, Borealis WB140HMS polypropylene homopolymer was used asthe primary polypropylene base resin. Braskem F020HC polypropylenehomopolymer was used as the secondary polypropylene base resin. Theresins were blended with Hydrocerol CF-40E as the primary nucleationagent, Heritage Plastics HT4HP talc as a secondary nucleation agent,Ampacet 102823 Process Aid PE MB LLDPE as a slip agent, Colortech11933-19 colorant, and N₂ as the blowing agent. The percentages were:

81.45%    Borealis WB140 HMS polypropylene homopolymer 15%  BraskemF020HC polypropylene homopolymer 0.05%   Hydrocerol CF-40E ChemicalBlowing Agent 2% Ampacet 102823 Process Aid PE MB LLDPE 1% Colortech11933-19 Titanium Oxide 0.5%  Heritage Plastics HT4HP Talc

The formulation was added to an extruder hopper. The extruder heated theformulation to form a molten resin mixture. The N₂ was injected at about0.074 lbs/hr into the resin blend to expand the resin and reducedensity.

The mixture thus formed was communicated to a co-extrusion die where themixture was extruded to form a core layer located between an outer skinlayer and an inner skin layer to establish a multi-layer parison. Themulti-layer parison was then blow molded with air to form a container.In one example, both the outer skin and the inner skin comprise apolypropylene resin. In another example, the outer skin was comprised ofDOW® DC 7067.00 polypropylene impact copolymer and the inner skin wascomprised of DOW® PP D207.03 developmental performance polypropyleneresin.

The multi-layer parison was then blow molded to form an insulativecellular non-aromatic polymeric bottle which had a bottle density ofabout 0.71 grams per cubic centimeter when and the core layer had adensity of about 0.677 grams per cubic centimeter.

Example 4 Formulation and Extrusion

In a core layer, Borealis WB140HMS polypropylene homopolymer was used asthe primary polypropylene base resin. Braskem F020HC polypropylenehomopolymer was used as the secondary polypropylene base resin. Theresins were blended with Hydrocerol CF-40E as the primary nucleationagent, Heritage Plastics HT4HP talc as a secondary nucleation agent,Ampacet 102823 Process Aid PE MB LLDPE as a slip agent, Colortech11933-19 colorant, and N₂ as the blowing agent. The percentages were:

81% Borealis WB140 HMS polypropylene homopolymer 15% Braskem F020HCpolypropylene homopolymer 0.5%  Hydrocerol CF-40E Chemical Blowing Agent 2% Ampacet 102823 Process Aid PE MB LLDPE  1% Colortech 11933-19Titanium Oxide 0.5%  Heritage Plastics HT4HP Talc

The formulation was added to an extruder hopper. The extruder heated theformulation to form a molten resin mixture. The N₂ was injected at about0.074 lbs/hr into the resin blend to expand the resin and reducedensity.

The mixture thus formed was communicated to a co-extrusion die where themixture was extruded to form a core layer located between an outer skinlayer and an inner skin layer to establish a multi-layer parison. Themulti-layer parison was then blow molded with air to form a container.In one example, both the outer skin and the inner skin comprise apolypropylene resin. In another example, the outer skin was comprised ofDOW® DC 7067.00 polypropylene impact copolymer and the inner skin wascomprised of DOW® PP D207.03 developmental performance polypropyleneresin.

The multi-layer parison was then blow molded to form an insulativecellular non-aromatic polymeric bottle which had a bottle density ofabout 0.69 grams per cubic centimeter when and the core layer had adensity of about 0.654 grams per cubic centimeter.

Example 5 Formulation and Extrusion

In a core layer, Borealis WB140HMS polypropylene homopolymer was used asthe primary polypropylene base resin. Braskem F020HC polypropylenehomopolymer was used as the secondary polypropylene base resin. Theresins were blended with Hydrocerol CF-40E as the primary nucleationagent, Heritage Plastics HT4HP talc as a secondary nucleation agent,Ampacet 102823 Process Aid PE MB LLDPE as a slip agent, Colortech11933-19 colorant, and N₂ as the blowing agent. The percentages were:

81% Borealis WB140 HMS polypropylene homopolymer 15% Braskem F020HCpolypropylene homopolymer 0.5%  Hydrocerol CF-40E Chemical Blowing Agent 2% Ampacet 102823 Process Aid PE MB LLDPE  1% Colortech 11933-19Titanium Oxide 0.5%  Heritage Plastics HT4HP Talc

The formulation was added to an extruder hopper. The extruder heated theformulation to form a molten resin mixture. The N₂ was injected at about0.1 lbs/hr into the resin blend to expand the resin and reduce density.

The mixture thus formed was communicated to a co-extrusion die where themixture was extruded to form a core layer located between an outer skinlayer and an inner skin layer to establish a multi-layer parison. Themulti-layer parison was then blow molded with air to form a container.In one example, both the outer skin and the inner skin comprise apolypropylene resin. In another example, the outer skin was comprised ofDOW® DC 7067.00 polypropylene impact copolymer and the inner skin wascomprised of DOW® PP D207.03 developmental performance polypropyleneresin.

The multi-layer parison was then blow molded to form an insulativecellular non-aromatic polymeric bottle which had a bottle density ofabout 0.53 grams per cubic centimeter when and the core layer had adensity of about 0.472 grams per cubic centimeter.

Example 6 Formulation and Extrusion

In a core layer, Borealis WB140HMS polypropylene homopolymer was used asthe primary polypropylene base resin. Braskem F020HC polypropylenehomopolymer was used as the secondary polypropylene base resin. Theresins were blended with Hydrocerol CF-40E as the primary nucleationagent, Heritage Plastics HT4HP talc as a secondary nucleation agent,Ampacet 102823 Process Aid PE MB LLDPE as a slip agent, Colortech11933-19 colorant, and N₂ as the blowing agent. The percentages were:

80.5%  Borealis WB140 HMS polypropylene homopolymer  15% Braskem F020HCpolypropylene homopolymer 1.0% Hydrocerol CF-40E Chemical Blowing Agent 2% Ampacet 102823 Process Aid PE MB LLDPE  1% Colortech 11933-19Titanium Oxide 0.5% Heritage Plastics HT4HP Talc

The formulation was added to an extruder hopper. The extruder heated theformulation to form a molten resin mixture. The N₂ was injected at about0.1 lbs/hr into the resin blend to expand the resin and reduce density.

The mixture thus formed was communicated to a co-extrusion die where themixture was extruded to form a core layer located between an outer skinlayer and an inner skin layer to establish a multi-layer parison. Themulti-layer parison was then blow molded with air to form a container.In one example, both the outer skin and the inner skin comprise apolypropylene resin. In another example, the outer skin was comprised ofDOW® DC 7067.00 polypropylene impact copolymer and the inner skin wascomprised of DOW® PP D207.03 developmental performance polypropyleneresin.

In one example, the multi-layer parison was then blow molded to form aninsulative cellular non-aromatic polymeric bottle which had a bottledensity of about 0.49 grams per cubic centimeter when and the core layerhad a density of about 0.427 grams per cubic centimeter. In anotherexample, the multi-layer parison was then blow molded to form aninsulative cellular non-aromatic polymeric bottle which had a bottledensity of about 0.54 grams per cubic centimeter when and the core layerhad a density of about 0.483 grams per cubic centimeter.

Example 7 Formulation and Extrusion

In a core layer, Borealis WB140HMS polypropylene homopolymer was used asthe primary polypropylene base resin. Braskem F020HC polypropylenehomopolymer was used as the secondary polypropylene base resin. Theresins were blended with Hydrocerol CF-40E as the primary nucleationagent, Heritage Plastics HT4HP talc as a secondary nucleation agent,Ampacet 102823 Process Aid PE MB LLDPE as a slip agent, Colortech11933-19 colorant, and N₂ as the blowing agent. The percentages were:

80.5%  Borealis WB140 HMS polypropylene homopolymer  15% Braskem F020HCpolypropylene homopolymer 1.0% Hydrocerol CF-40E Chemical Blowing Agent 2% Ampacet 102823 Process Aid PE MB LLDPE  1% Colortech 11933-19Titanium Oxide 0.5% Heritage Plastics HT4HP Talc

The formulation was added to an extruder hopper. The extruder heated theformulation to form a molten resin mixture. The N₂ was injected at about0.1 lbs/hr into the resin blend to expand the resin and reduce density.

The mixture thus formed was communicated to a co-extrusion die where themixture was extruded to form a core layer located between an outer skinlayer and an inner skin layer to establish a multi-layer parison. Themulti-layer parison was then blow molded with air to form a container.In one example, both the outer skin and the inner skin comprise apolyethylene resin. In another example, both the outer skin and theinner skin were comprised of high density ethylene hexane-1 copolymer(Chevron Phillips Marlex® HHM 5502 BN).

In one example, multi-layer parison was then blow molded to form aninsulative cellular non-aromatic polymeric bottle which had a bottledensity of about 0.49 grams per cubic centimeter when and the core layerhad a density of about 0.427 grams per cubic centimeter.

Example 8

Density Measurements

This Example demonstrates the test used to measure the density of filledand unfilled polymer parts.

Procedure

The density was determined by the apparatus shown, unassembled, inFIG. 1. Although not shown in FIG. 1, the apparatus also included athermometer to measure the suspension liquid temperature. A suspensionliquid is a fluid with a density lower than that of the sample to bemeasured. The sample must sink in the suspension fluid to determine thesample density. Water has a density of 1 g/cm3, so most unfilledpolymers require some other suspension fluid such as isopropyl alcohol,density=0.8808 g/cm3. A Mettler AT400 balance (Mettler-Toledo LLC,Columbus, Ohio) was also used.

The density of a limestone-filled HDPE bottle was measured. After taringthe balance to zero, the dry solid sample was weighed after placing itin the cup of the Mettler balance. The dry weight was 0.3833 g. Afterweighing the dry sample and before removing the sample from the cup, thebalance was tared again. The sample was removed from the cup and placedon the gem holder in the suspension fluid. The sample was weighedproviding the weight with a negative number (−0.3287 g). The number wasconverted to its absolute value (0.3287 g); the positive value is thesample buoyancy. The sample density was calculated by multiplying thedry weight (0.3833 g) by the sample buoyancy (0.3287 g) by thesuspension fluid density (0.8808 g/cc), which equaled 1.0272 g/cc.

1. A container comprising a first layer and a core layer comprising aninsulative cellular non-aromatic polymeric material comprising at leastone polypropylene resin that is at least 85 wt % of the insulativecellular non-aromatic polymeric material, at least one nucleating agentthat is up to about 15 wt % of the insulative cellular non-aromaticpolymeric material, and wherein the first layer has been extruded ontothe core layer so that the core layer and the first layer are in directcontact.
 2. The container of claim 1, wherein the polypropylene resin isa polypropylene copolymer.
 3. The container of claim 1, wherein thepolypropylene resin is a polypropylene homopolymer.
 4. The container ofclaim 1, wherein the at least one polypropylene resin is two differentpolypropylene resins.
 5. The container of claim 4, wherein the ratio ofthe two different polypropylene resins is 50% to 50%.
 6. The containerof claim 1, wherein the at least one polypropylene resin is about 90 to99.9 wt % of the insulative cellular non-aromatic polymeric material. 7.The container of claim 6, wherein the at least one polypropylene resinis about 95 to 99.9 wt % of the insulative cellular non-aromaticpolymeric material.
 8. The container of claim 7, wherein the at leastone polypropylene resin is about 96 wt % of the insulative cellularnon-aromatic polymeric material.
 9. The container of claim 1, whereinthe at least one nucleating agent is about 0.1 to 5 wt % of theinsulative cellular non-aromatic polymeric material.
 10. The containerof claim 9, wherein the at least one nucleating agent is about 0.5 to 5wt % of the insulative cellular non-aromatic polymeric material.
 11. Thecontainer of claim 1, wherein the insulative cellular non-aromaticpolymeric material further comprises regrind of the insulative cellularnon-aromatic polymeric material.
 12. The container of claim 1, whereinthe insulative cellular non-aromatic polymeric material furthercomprises a slip agent that is up to about 3 wt % of the insulativecellular non-aromatic polymeric material.
 13. The container of claim 1,wherein the at least one nucleating agent is up to 2 wt % of theinsulative cellular non-aromatic polymeric material.
 14. The containerof claim 13, wherein the nucleating agent is about 0.1 to 0.5 wt % ofthe insulative cellular non-aromatic polymeric material.
 15. Thecontainer of claim 1, wherein the insulative cellular non-aromaticpolymeric material lacks talc.
 16. The container of claim 1, wherein thecontainer has a density of about 0.5 g/cm3 to about 0.8 g/cm3.
 17. Thecontainer of claim 1, wherein the outer layer is a solid layer having adensity of about 0.9 g/cm3.
 18. The container of claim 1, wherein the atleast one polypropylene resin includes regrind.
 19. The container ofclaim 1, wherein the insulative cellular non-aromatic material furtherincludes a blowing agent.
 20. The container of claim 1, wherein theouter layer comprises polypropylene.